@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_head { this: np:hasAssertion dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_assertion; np:hasProvenance dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_provenance; np:hasPublicationInfo dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_publicationInfo; a np:Nanopublication . dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_assertion a np:Assertion . dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_provenance a np:Provenance . dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_publicationInfo a np:PublicationInfo . } dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_assertion { miriam-gene:2147 a ncit:C16612 . lld:C0398625 a ncit:C7057 . dgn-gda:DGNe091ac3f3ee2c2a8788db421cec596bb sio:SIO_000628 miriam-gene:2147, lld:C0398625; a sio:SIO_001122 . } dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_provenance { dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_assertion dcterms:description "[The following frequencies (patients v controls), odds ratios (ORs), and confidence intervals (CIs) of single risk factors were found: Lp(a) >30 mg/dL (26.4% v 4.7%; OR/CI, 7.2/3.8 to 13.8; P <.0001), FV G1691A (20.2% v 4%; OR/CI, 6/2.97 to 12.1; P <.0001), protein C deficiency (6% v 0.67%; OR/CI, 9.5/2 to 44.6; P =.001), PT G20210A (6% v 1.3%; OR/CI, 4.7/1.4 to 15.6; P =.01), and the MTHFR TT677 genotype (23.6% v 10.4%; OR/CI, 2.4/1.53 to 4.5; P <.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:10572079; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP268325.RAXdfcezBH77sSi6UyMiZywmHFZbgR4t8q1NHeS4eAHt8130_publicationInfo { this: dcterms:created "2016-05-13T12:43:47+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }